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Table 3 Hereditary demographics, risk factors, and tumor characteristics

From: Analysis of the pathogenic variants of BRCA1 and BRCA2 using next-generation sequencing in women with familial breast cancer: a case–control study

Variable

BRCA mutation carriers n = 21

Non-carriers n = 80

 

Age: m (SD)

35.6 (4.5)

37.3 (5.4)

p = 0.18

Family history of cancer

66.6%

50.0%

p = 0.17

Body mass index, m (SD)

27.8 (5.0)

27.7 (5.5)

p = 0.94

Age at menarche m (SD)

12.1 (2.9)

12.1 (1.7)

p = 1.00

No. pregnancy m (SD)

2.4 (2.1)

2.3 (1.5)

p = 0.80

Nulligravid (%)

19.0%

17.7%

p = 0.89

Age at first birth, m (SD)

20.7 (4.9)

21.6 (5.6)

p = 0.50

Breastfeeding %

35.2%

59.3%

p = 0.04

Contraception (%)

40%

37.9%

p = 0.86

Smoking (%)

14.2%

17.5%

p = 0.72

Histology, ductal. (%)

88%

89%

p = 0.90

Nuclear grade. (%)

 2

27%

41.5%

p = 0.28

 3

67%

49.2%

p = 0.22

Stage. (%)

 0

4.7%

0%

p = 0.0002

 I-II

71.4%

52.5%

p = 0.12

 III

23.8%

42.5%

p = 0.11

 IV

0%

5%

p = 0.29

T

 0–1

19%

31.6%

p = 0.26

 2

57%

31.6%

p = 0.03

 3

19%

26.6%

p = 0.47

 4

4.7%

10.2%

p = 0.43

N Positive

50%

62%

p = 0.33

 IHC

 ER (+)

30%

60.5%

p = 0.01

 PR (+)

30%

53.9%

p = 0.058

 HER (+)

16%

21.6%

p = 0.57

 Triple Negative.

65%

22.6%

p = < 0.001

  1. m mean, SD standard deviation, IHC immunohistochemical analysis, ER estrogen receptor, PR progesterone receptor